A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759644



Internal ID20535505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27533727..27533727hg38UCSC Ensembl
chr13:28107864..28107864hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759644
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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